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rs587776605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776605(-;-)
Make rs587776605(-;GT)
Make rs587776605(GT;GT)
ReferenceGRCh38 38.1/142
Chromosome2
Position144403963
GeneZEB2
is asnp
is mentioned by
dbSNPrs587776605
ebirs587776605
HLIrs587776605
Exacrs587776605
Varsomers587776605
Maprs587776605
PheGenIrs587776605
hapmaprs587776605
1000 genomesrs587776605
hgdprs587776605
ensemblrs587776605
gopubmedrs587776605
geneviewrs587776605
scholarrs587776605
googlers587776605
pharmgkbrs587776605
gwascentralrs587776605
openSNPrs587776605
23andMers587776605
23andMe allrs587776605
SNP Nexus

SNPshotrs587776605
SNPdbers587776605
MSV3drs587776605
GWAS Ctlgrs587776605
Max Magnitude0
ClinVar
Risk rs587776605(GT;GT)
Alt rs587776605(GT;GT)
Reference rs587776605(;)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 0
HGVS NC_000002.11:g.145161529_145161530dupGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000005024.2,